Familial hemophagocytic lymphohistiocytosis 2

MONDO:0011337

Any genetic hemophagocytic lymphohistiocytosis in which the cause of the disease is a mutation in the PRF1 gene.

Also known as: FHL2, HLH2, HPLH2, PRF1 genetic hemophagocytic lymphohistiocytosis, familial hemophagocytic lymphohistiocytosis type 2, genetic hemophagocytic lymphohistiocytosis caused by mutation in PRF1, hemophagocytic lymphohistiocytosis, familial, type 2, Hlh2

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